PDCD10 anticorps

N° du produit ABIN6568687

Détail du produit anti-PDCD10 anticorps

Antigène: PDCD10 (Programmed Cell Death 10 (PDCD10))

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp PDCD10 est non-conjugé

Application: Western Blotting (WB)

Purification: Affinity purification

Immunogène: Recombinant protein of human PDCD10

Isotype: IgG

Information d'application

Indications d'application: WB 1:200 - 1:2000

Restrictions: For Research Use only

Stockage

Concentration: 1 mg/mL

Buffer: Buffer: PBS with 0.02 % sodium azide, 50 % glycerol,  pH 7.3.

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: -20 °C

Stockage commentaire: Store at -20°C. Avoid freeze / thaw cycles.

Détails sur PDCD10

Antigène: PDCD10 (Programmed Cell Death 10 (PDCD10))

Autre désignation: PDCD10 (PDCD10 Produits)

Synonymes: anticorps CCM3, anticorps TFAR15, anticorps 2410003B13Rik, anticorps Ccm3, anticorps Tfa15, anticorps Tfar15, anticorps zgc:85629, anticorps ccm3a, anticorps pdcd10, anticorps zgc:65826, anticorps programmed cell death 10, anticorps programmed cell death 10 S homeolog, anticorps programmed cell death 10b, anticorps programmed cell death 10a, anticorps PDCD10, anticorps Pdcd10, anticorps pdcd10.S, anticorps pdcd10b, anticorps pdcd10a

Sujet:

Synonyms: Apoptosis related protein 15,CCM3,Cerebral cavernous malformations 3 protein,MGC1212,MGC24477,PDC10,PDCD 10,PDCD10,Programmed cell death 10,Programmed cell death protein 10,TF 1 cell apoptosis related protein 15,TF-1 cell apoptosis-related protein 15,TFAR15

Background: This gene encodes an evolutionarily conserved protein associated with cell apoptosis. The protein interacts with the serine/threonine protein kinase MST4 to modulate the extracellular signal-regulated kinase (ERK) pathway. It also interacts with and is phosphoryated by serine/threonine kinase 25, and is thought to function in a signaling pathway essential for vascular developent. Mutations in this gene are one cause of cerebral cavernous malformations, which are vascular malformations that cause seizures and cerebral hemorrhages. Multiple alternatively spliced variants, encoding the same protein, have been identified.

Poids moléculaire:

Observed_MW: 26kDa

Calculated_MW: 24kDa

ID gène: 11235

UniProt: Q9BUL8